- Home
- Materials
Filter
Sort
-
-
Filter Clear filters
-
-
Scientific topic
- Applied ontology1
- Biomedical informatics1
- Clinical informatics1
- Cloud computing1
- Computer science1
- Data management1
- FAIR data1
- Findable, accessible, interoperable, reusable data1
- HPC1
- Health and disease1
- Health informatics1
- Healthcare informatics1
- High performance computing1
- High-performance computing1
- Medical informatics1
- Metadata management1
- Ontologies1
- Ontology1
- Ontology and terminology1
- Ontology relations1
- Research data management (RDM)1
- Terminology1
- Upper ontology1
- Show N_FILTERS more
-
-
-
Operation
- Data editing
- Data handling48
- File handling48
- File processing48
- Processing48
- Report handling48
- Utility operation48
- Data extraction13
- Data retrieval13
- Data retrieval (metadata)13
- Metadata retrieval13
- Retrieval13
- Data analysis10
- Mathematical modelling8
- Modelling and simulation8
- Data brokering7
- Data deposition7
- Data deposition brokering7
- Data submission7
- Database deposition7
- Database submission7
- Data visualisation6
- Molecular visualisation6
- Plotting6
- Rendering6
- Visualisation6
- Database retrieval5
- Query5
- Query and retrieval5
- Annotation2
- Database search2
- Normalisation2
- Ontology browsing2
- Ontology visualisation2
- RNA-Seq analysis2
- Search2
- Standardisation2
- Standardisation and normalisation2
- Alignment1
- Alignment construction1
- Alignment generation1
- Allele calling1
- Biological network analysis1
- Biological network modelling1
- Biological network prediction1
- Comparison1
- Data formatting1
- Data reformatting1
- Exome variant detection1
- File format conversion1
- File formatting1
- File reformatting1
- Format conversion1
- Genome variant detection1
- Germ line variant calling1
- Image analysis1
- Mutation detection1
- Network analysis1
- Network comparison1
- Network modelling1
- Network prediction1
- Network simulation1
- Network topology simulation1
- Quality control1
- Read pre-processing1
- Sequence generation1
- Sequence generation (nucleic acid)1
- Sequence generation (protein)1
- Sequence read pre-processing1
- Somatic variant calling1
- Validation1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
- Show N_FILTERS more
-
-
-
Content provider
- Swiss Institute of Bioinformatics1
- Show N_FILTERS more
-
-
-
Difficulty level
- Beginner1
- Show N_FILTERS more
-
-
-
Contributor
- Kristin Gnodke1
- Sabine Österle1
- Show N_FILTERS more
-
-
-
Resource type
- E-learning1
- Training materials1
- Video1
- Show N_FILTERS more
-
- Show disabled materials
- Hide archived materials
